部分構造検索

CCN(CC)CC(C)N

COc1ccc2sc(C(=N)C(C#N)N3CCN(C(=O)c4ccccc4)C[C@H]3C)nc2c1
Reaction #7696
(R)-N-(benzoyl)-3-methyl-N′-[2-(5-methoxy-benzothiazol-2-yl)-2-imino-1-cyano-ethyl]-piperazine
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1NC(=O)[C@H](C)N(Cc2ccc(F)cc2)C1=O
Reaction #11703
title compound
収率 23.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN[C@@H](C)CN1Cc1ccc(F)cc1
Reaction #11704
title compound
収率 90.6%DOI: 10.6084/m9.figshare.5104873.v1
COCCN1CC(c2cccc(F)c2F)CC(NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #48454
title compound
収率 42.7%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@H]1CCCN(C2CCCCC2(O)C(C)c2cccc(OC(F)(F)F)c2)C1.Cl.Cl
Reaction #57101
2-[(3S)-3-(methylamino)piperidin-1-yl]-1-[3-(trifluoromethoxy)phenyl]ethylcyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(Oc3cccc(-c4cnc(C5CCCN5C(=O)C(NC(=O)OC)C(C)C)[nH]4)c3)cc2)[nH]1)C(C)C
Reaction #158863
[1-(2-{5-[4-(3-{2-[1-(2-Methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-phenoxy)-phenyl]-1H-imidazol-2-yl}-pyrrolidine-1-carbonyl)-2-methyl-propyl]-carbamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc3c(c2)Cc2cc(-c4cnc(C5CCCN5C(=O)C(NC(=O)OC)C(C)C)[nH]4)ccc2-3)[nH]1)C(C)C
Reaction #158873
(1-{2-[5-(7-{2-[1-(2-Methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-9H-fluoren-2-yl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1CNC(=O)c1ccc(-c2ccc(-c3cnc(C4CCCN4C(=O)C(NC(=O)OC)C(C)C)[nH]3)cc2)cc1)C(C)C
Reaction #158903
[1-(2-{[(4′-{2-[1-(2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-biphenyl-4-carbonyl)-amino]-methyl}-pyrrolidine-1-carbonyl)-2-methyl-propyl]-carbamic acid methyl ester
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](C(=O)N1CCCC1c1ncc(-c2ccc(-c3ccc(-c4cnc(CN5CCCC(N)C5=O)[nH]4)cc3)cc2)[nH]1)C(C)C
Reaction #158926
(R)-{1-[2-(5-{4′-[2-(3-amino-2-oxo-piperidin-1-ylmethyl)-3H-imidazol-4-yl]-biphenyl-4-yl}-1H-imidazol-2-yl)-pyrrolidine-1-carbonyl]-2-methyl-propyl}-carbamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(-c3ccc(-c4cnc(CN5CCC[C@@H](NC(=O)OC)C5=O)[nH]4)cc3)cc2)[nH]1)C(C)C
Reaction #158927
(R)-{1-[5-(4′-{2-[1-(2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-biphenyl-4-yl)-1H-imidazol-2-ylmethyl]-2-oxo-piperidin-3-yl}-carbamic acid methyl ester
収率 319.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC1CCC2CCC(c3ncc(-c4ccc(-c5ccc(-c6cnc(C7CCCN7C(=O)C(NC(=O)OC)C(C)C)[nH]6)cc5)cc4)[nH]3)N2C1=O
Reaction #158928
{3-[5-(4′-{2-[1-(2-Methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-biphenyl-4-yl)-1H-imidazol-2-yl]-5-oxo-octahydro-indolizin-6-yl}-carbamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC1CCCN(C(C)C(=O)NCC(=O)c2ccc(-c3ccc(-c4cnc(C5CCCN5C(=O)C(NC(=O)OC)C(C)C)[nH]4)cc3)cc2)C1=O
Reaction #158938
(1-{1-[2-(4′-{2-[1-(2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-biphenyl-4-yl)-2-oxo-ethylcarbamoyl]-ethyl}-2-oxo-piperidin-3-yl)-carbamic acid methyl ester
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(-c3ccc(-c4cnc(C5SCCN5C(=O)C(NC(=O)OC)C(C)C)[nH]4)cc3)cc2)[nH]1)C(C)C
Reaction #159067
(1-{2-[5-(4′-{2-[1-(2-Methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-biphenyl-4-yl)-1H-imidazol-2-yl]-thiazolidine-3-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1nc(-c2ccc3cc(-c4ccc(C(=O)CNC(=O)C5CC(c6ccccc6)CN5C(=O)OC(C)(C)C)cc4)ccc3c2)c[nH]1)C(C)C
Reaction #159140
crude material
収率 174.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1ncc(-c2ccc(-c3ccc4cc(-c5cnc(C6CC(C#N)CN6)[nH]5)ccc4c3)cc2)[nH]1)C(C)C.Cl.Cl.Cl
Reaction #159156
title compound
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC(C#N)CC1c1ncc(-c2ccc3cc(-c4ccc(-c5cnc(C6CC7(CC7)CN6C(=O)C(NC(=O)OC)C(C)C)[nH]5)cc4)ccc3c2)[nH]1)C(C)C
Reaction #159157
title compound
収率 11.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)OC)C(=O)N1CC(C#N)CC1c1ncc(-c2ccc3cc(-c4ccc(-c5cnc(C6CC7(CC7)CN6C(=O)C(NC(=O)OC)C(C)C)[nH]5)cc4)ccc3c2)[nH]1
Reaction #159158
title compound
収率 54.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1ncc(-c2ccc(-c3ccc4cc(-c5cnc(C6CC(C#N)CN6C(=O)C(NC(=O)OC)C(C)(C)C)[nH]5)ccc4c3)cc2)[nH]1)C(C)C
Reaction #159159
title compound
収率 48.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1ncc(-c2ccc3cc(-c4ccc(-c5cnc(C6CC(C#N)CN6)[nH]5)cc4)ccc3c2)[nH]1)C(C)C.Cl.Cl.Cl
Reaction #159161
title compound
収率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(=O)OC)C(=O)N1CC(C#N)CC1c1ncc(-c2ccc(-c3ccc4cc(-c5cnc(C6CC7(CC7)CN6C(=O)C(NC(=O)OC)C(C)C)[nH]5)ccc4c3)cc2)[nH]1
Reaction #159162
title compound
収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
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